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Projects / Programmes source: ARIS

Prognostic and predictive factors for response in treatment of different types of cancer

Periods
Research activity

Code Science Field Subfield
3.04.00  Medical sciences  Oncology   

Code Science Field
B007  Biomedical sciences  Medicine (human and vertebrates) 

Code Science Field
3.02  Medical and Health Sciences  Clinical medicine 
Keywords
sequencing of the new generation, liquide biopsy, predictive and prognostic factors, predictive response factor for treatment, different types of cancer
Evaluation (rules)
source: COBISS
Points
5,305.56
A''
319.81
A'
1,163.11
A1/2
2,094.94
CI10
16,601
CImax
1,983
h10
49
A1
16.55
A3
49.63
Data for the last 5 years (citations for the last 10 years) on September 24, 2023; A3 for period 2017-2021
Data for ARIS tenders ( 04.04.2019 – Programme tender , archive )
Database Linked records Citations Pure citations Average pure citations
WoS  657  16,728  16,193  24.65 
Scopus  539  19,132  18,576  34.46 
Researchers (23)
no. Code Name and surname Research area Role Period No. of publicationsNo. of publications
1.  14114  PhD Darja Arko  Medical sciences  Researcher  2020 - 2023  317 
2.  16303  PhD Simona Borštnar  Medical sciences  Researcher  2020 - 2023  466 
3.  20133  Nina Čas Sikošek  Medical sciences  Technical associate  2020 - 2023  84 
4.  53393  Eva Erzar  Medical sciences  Junior researcher  2020 - 2023 
5.  32509  Kristina Gornik Kramberger  Medical sciences  Technical associate  2021 - 2023  42 
6.  15875  PhD Cvetka Grašič Kuhar  Medical sciences  Researcher  2020 - 2023  231 
7.  12022  PhD Barbara Jezeršek Novaković  Medical sciences  Researcher  2020 - 2023  321 
8.  10772  PhD Rajko Kavalar  Medical sciences  Researcher  2020  247 
9.  12224  PhD Borut Kragelj  Medical sciences  Researcher  2020 - 2023  78 
10.  51959  PhD Damjan Manevski  Medical sciences  Researcher  2022 - 2023  38 
11.  34225  PhD Tanja Marinko  Medical sciences  Researcher  2020 - 2023  159 
12.  20055  PhD Erika Matos  Medical sciences  Researcher  2020 - 2023  177 
13.  32614  PhD Tanja Mesti  Medical sciences  Researcher  2020 - 2023  173 
14.  51035  Milena Mikluš  Medical sciences  Technical associate  2021 
15.  13541  PhD Janja Ocvirk  Medical sciences  Head  2020 - 2023  794 
16.  54719  Matej Panjan  Medical sciences  Junior researcher  2020 - 2023 
17.  55823  Tina Pavlin  Medical sciences  Junior researcher  2021 - 2023 
18.  20056  PhD Martina Reberšek  Medical sciences  Researcher  2020 - 2023  256 
19.  33230  PhD Nina Ružić Gorenjec  Natural sciences and mathematics  Researcher  2020 - 2021  47 
20.  24577  PhD Boštjan Šeruga  Medical sciences  Researcher  2020 - 2023  289 
21.  01324  PhD Iztok Takač  Medical sciences  Researcher  2020 - 2023  891 
22.  52993  Aljaž Valič  Social sciences  Technical associate  2021 - 2023  18 
23.  11747  PhD Branko Zakotnik  Medical sciences  Retired researcher  2020 - 2021  420 
Organisations (3)
no. Code Research organisation City Registration number No. of publicationsNo. of publications
1.  0302  Institute of Oncology Ljubljana  Ljubljana  5055733000  14,834 
2.  0334  University Medical Centre Maribor  Maribor  5054150000  22,673 
3.  0381  University of Ljubljana, Faculty of Medicine  Ljubljana  1627066  45,607 
Abstract
At the Institute of Oncology Ljubljana are treated patients with different types of tumors, using also the new treatment modalities, including targeted drugs and immunotherapy. This research program will continue to explore already established and develop new prognostic and predictive factors that can predict the response to the treatment. This will help us in finding the best personalized approach to every patient and offer the optimal treatment to each individual cancer patient. Knowing the biomarkers status in patients with various cancers can give us information about the course of the disease and the response to the treatment. Early discovery of a disease recidive or progression enables oncologists for early treatment and therapeutic strategy change when we can catch the disease while in a smaller scale and the patient in a better condition. Consequently a longer survival of the patient will be achieved. For this aim, genetic analyzes of cancerous tissue and / or body liquids assessed with next generation sequencing will be incorporated. Sequencing of target genes can determine various genetic changes or mutations, and change of the molecular profile of the disease in the course of the treatment or in the case of disease progression. Different gene mutations are more typical for certain cancers and their treatment, and they also show the different organic affinity of cancer cells for breeding. The next generation sequencing is a new tool, already validated and highly sensitive to detect the changes in the dynamics of the disease or changes in the molecular profile of the disease very early and can provide data for the simultaneous detection and identification of fusions, point mutations, and the expression level of more than hundred genes specific to different cancers. Here we will develop some new potential biomarkers that can predict the affinity of the cancer cells for breading, like the presence of gene mutations for Tropomyosin receptor kinase (NTRK1, NTRK2, NTRK3) that indicate affinity for the brain, with a poor prognosis or high expression of interferon alpha (IFN) genes, assessed by Interferon Gamma Messenger RNA Signature, that can be a predictive factor for a better response to immunotherapy (PD1 / PDL1 inhibitors). New knowledge and new tumor biomarkers will be eventually implemented in treatment of cancer patients in Slovenia.
Significance for science
Due to better understanding of the biology of cancer many new effective anticancer agents were approved in recent years. In oncology we strive for the personalized approach. With this approach we aim to treat every individual cancer patient with the most effective and at the same time the least toxic therapy. To reach this goal it is important to know prognostic factors and predictive factors for response to a particular anticancer therapy. Furthermore, it is also important to understand predictive factors for for the development of early and late toxic effects related to anticancer treatment. The biggest advancement in treatment of cancer are targeted agents and the immunotherapy. These drugs are the most effective in cancers with dominant signalling pathways, which are crucial for growth of tumor (e.g. cetuximab targeting EGFR in EGFR positive metastatic colorectal cancer, trastuzumab targeting HER-2 in HER-2 positive breast cancer, imatinib targeting Bcr-Abl fusion protein in chronic myeloic leukemia or gefitinib targeting the activating mutation of EGFR in non-small cell lung cancer). In these cancers biomarkers are available, which predict response to these agents. Unfortunatelly, not all targeted agents are like this. Although they are called targeted agents for many of them actually we do not know the corresponding targets within cancer cells or they are targeting pathways which are not dominant. Consequently, there are no predictive biomarkers available for them. An examplele of such drugs are mTOR inhibitors, which are used for treatment of patients with advanced renal cell carcinoma or VEGF inhibitors used in advanced colorectal cancer. Before the start of therapy with mTOR or VEGF inhibitors we cannot predict which patients will benefit from these drugs. However, most of the patients who receive these drugs develop toxic effects, some life-threatening side effects.Therefore, it is of paramount importance to identify predictive biomarkers for response to these and other similar drugs. We also need to identify new prognostic biomarkers (e.g. NTRK1, NTRK2, NTRK3 ), which could potentially serve as targets for the development of new and more effective therapies, and in the same time can predict the cancer cells breeding afinity for different organs, esspecially for the CNS. Interferon Gamma Messenger RNA Signature is a predictive factor for a better response to immunotherapy (PD1 / PDL1 inhibitors). Increased intensity of interferon alpha (IFN) genes can be determined by IFN signature - Interferon Gamma Messenger RNA Signature. Early discovery of a disease recidive or progression enables oncologists for early treatment and therapeutic strategy change when we can catch the disease while in a smaller scale and the patient in a better condition. Consequently a longer survival of the patient should be acchieved. Genetic analyzes of cancerous tissue and / or body liquids with the next generation sequencing, can predict changes in the dynamics of the disease or changes in the molecular profile of the disease very early. The burden of circulating tumor DNA (cDNA) is an early negative predictive factor. Sequencing of target genes can determine various genetic changes or mutations, and change of the molecular profile of the disease in the course of treatment or in the case of disease progression. Different gene mutations are more typical for certain cancers and their treatment, and they also show the different organic affinity of cancer cells for breeding.
Significance for the country
The goal of the contemporary oncologic treatment is thepersonalized approach, which allows every individual patient the most effective and at the same time the least toxic treatment. With better understanding of prognostic and predictive factors we can further improve currently available personalized approach. In an individual patient we aim to improve a chance of cure and to minimize acute and chronic toxic effects of therapy. A higher proportion of cured patients who experience minimal late side effects of treatment could contribute to increased power of our State. Not only an individual but the whole community can benefit by this approach. The average monthly cost of new anticancer systemic therapies for an individual patient is several thousand of euros. However, many patients who are treated with these new agents do not benefit from them. In current situation of the economic crisis costs of anticancer treatment are becoming unsustainable. With better tailored personalized treatment approach we could substantially decrease the costs of oncologic treatment.   Results of our studies will be published in international journals and presented at interanational scientific meetings, which can increase the visibility of Slovenia around the world. Our research studies will enable even more intensive integration of Slovenian researchers into the interantional scientific community. In Slovenia, our research program will contribute fo a faster introduction of modern methods in routine practice and to improved professional quality. During program implementation we will ensure education and training of students and other people in training.
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